Magnetic Resonance Imaging of Brain Anomalies in Fetal Alcohol Syndrome von Swayze, Victor W., II, Johnson, Virginia P, Hanson, James W, Piven, Joseph, Sato, Yutaka, Giedd, Jay N, Mosnik, Diane, Andreasen, Nancy C

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Areas of Triangles and other Polygons with Vertices from Various Sequences von Johnson, Virginia P., Cook, Charles K.

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Correlation of severity and outcome with plasma sterol levels in variants of the Smith-Lemli-Opitz syndrome von Tint, G.S., Salen, Gerald, Batta, Ashok K., Shefer, Sarah, Irons, Mira, Elias, Ellen Roy, Abuelo, Dianne N., Johnson, Virginia P., Lambert, Marie, Lutz, Richard, Schanen, Carolyn, Morris, Colleen A., Hoganson, George, Hughes-Benzie, Rhiannon

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Linkage of a Human Brain Malformation, Familial Holoprosencephaly, to Chromosome 7 and Evidence for Genetic Heterogeneity von Muenke, Maximilian, Gurrieri, Fiorella, Bay, Carolyn, Yi, David H., Collins, Amanda L., Johnson, Virginia P., Raoul C. M. Hennekam, Schaefer, G. Bradley, Weik, LuAnn, Lubinsky, Mark S., Daack-Hirsch, Sandy, Moore, Cynthia A., Dobyns, William B., Murray, Jeffrey C., Price, R. Arlen

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Uniparental isodisomy of chromosome 14 in two cases: An abnormal child and a normal adult von Papenhausen, Peter R., Mueller, O. Thomas, Johnson, Virginia P., Sutcliffe, Maxine, Diamond, Theresa M., Kousseff, Boris G.

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Fetal Alcohol Syndrome: A Guide for Families and Communities von JOHNSON, VIRGINIA P.

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Natural history of mosaic trisomy 14 syndrome von Fujimoto, Atsuko, Allanson, Judith, Crowe, Carol A., Lipson, Mark H., Johnson, Virginia P.

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A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism von Johnson, Virginia P., McMillin, J. Michael, Aceto Jr, Thomas, Bruins, George, John M.

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Smith-Lemli-Opitz syndrome: Review and report of two affected siblings von Johnson, Virginia P.

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Alpha-fetoprotein and acetylcholinesterase in twins discordant for neural tube defect von Johnson, Virginia P., Vidgoff, Jaclyn, Wilson, Nancy, Madison, Dean

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Fetal alcohol syndrome: Craniofacial and central nervous system manifestations von Johnson, Virginia P., Swayze II, Victor W., Sato, Yutaka, Andreasen, Nancy C.

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Holoprosencephaly: A developmental field defect von Johnson, Virginia P.

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Duplication of the distal part of the long arm of chromosome 1 von Johnson, Virginia P.

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Duplication 10q confirmed by DNA in situ hybridization von Johnson, Virginia P., Sutliff, Willis C.

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Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs von Altherr, Michael R., Wright, Tracy J., Denison, Karen, Perez-Castro, Ana V., Johnson, Virginia P.

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FISH detection of Wolf-Hirschhorn syndorem: Exclusion of D4F26 as critical site von Johnson, Virginia P., Altherr, Michael R., Blake, Jerome M., Keppen, Laura D.

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Uniparental isodisomy of chromosome 14 in two cases: An abnormal child and a normal adult von Papenhausen, Peter R., Mueller, O. Thomas, Sutcliffe, Maxine, Diamond, Theresa M., Kousseff, Boris G., Johnson, Virginia P.

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Distinct 15q genotypes in Russell-Silver and ring 15 syndromes von Rogan, Peter K., Seip, James R., Driscoll, Daniel J., Papenhausen, Peter R., Johnson, Virginia P., Raskin, Salmo, Woodward, Amy L., Butler, Merlin G.

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Deletion of the distal long arm of chromosome 1: A definable syndrome von Johnson, Virginia P., Heck, Louis J., Carter, Guy A., Flom, Jon O., Opitz, John M., Reynolds, James F.

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Molecular detection of a 4p deletion using PCR-based polymorphisms: A technique for the rapid detection of the Wolf-Hirschhorn syndrome von Altherr, Michael R., Gusella, James F., Wasmuth, John J., Kummer, Mark A., McKercher, Scott W., Johnson, Virginia P.

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